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Using a Diabetes Registry to Improve Care & Outcomes Judith A. Cook, Ph.D. Professor & Director UIC Center on Psychiatric Disability & Occurring Medical Conditions Collaborative Support Programs of
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A diabetes registry is a database or system that collects and maintains information about individuals with diabetes.
Healthcare providers and organizations that treat individuals with diabetes are required to file using a diabetes registry.
Healthcare providers can fill out using a diabetes registry by entering relevant information about their patients with diabetes into the system.
The purpose of using a diabetes registry is to track and monitor the health outcomes of individuals with diabetes, as well as to improve care and treatment for this population.
Information such as patient demographics, lab results, medications, and treatment plans must be reported on using a diabetes registry.
The deadline to file using a diabetes registry in 2023 is typically at the end of the calendar year, but specific deadlines may vary depending on the organization or jurisdiction.
The penalty for late filing of using a diabetes registry may vary by jurisdiction, but it could include fines or other disciplinary actions against the healthcare provider or organization.
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